Table 6.
Hybrid nanoformulation
Diseases | Antiviral drug | Type of nanodelivery system | Lipid and polymer which used as carrier | Problems encountered | Key findings | Ref |
---|---|---|---|---|---|---|
HIV/AIDS | Zidovudine | Lipid–polymer hybrid nanoparticles |
Stearic acid, Compritol 888 ATO, polymer Gelatin |
Low aqueous solubility Short half-life and high side effects |
High loading, hemocompatibility, sustained release | [232] |
HIV/AIDS | Zidovudine | Lipid–polymer hybrid nanoparticles | Alginate, stearic acid, PEG | Biocompatibility problems, high toxicity | Biocompatibility, superior drug-loading capacity, and enhanced drug release efficacy | [233] |
HIV/AIDS | Nevirapine | Lipid–polymer hybrid nanoparticles | PEG 400, propylene glycol, polyoxyethylene polyoxypropylene (copolymer), glyceryl monostearate, polyglyceryl distearate | Decreased solubility | Increased drug delivery to target sites | [233] |
HIV/AIDS | Zidovudine | Core shell nanoparticle | Long-chain fatty acid, stearic acid, PEG, dextran | Biodegradability and biocompatibility | High stability, controlled drug release | [234] |
HIV/AIDS | Zidovudine | Core shell nanoparticle | PVP, stearic acid, PEG |
Short half-life Low bioavailability |
Decreased systemic side effects, useful therapeutic activity | [235] |